目錄:MedChemExpress LLC>>生化試劑>> DTP3 TFA | MCE
純度 | 98.03% | 分子量 | 639.62 |
---|---|---|---|
分子式 | C??H??F?N?O? | 供貨周期 | 現(xiàn)貨 |
規(guī)格 | 5 mg | 貨號 | HY-100538A |
應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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CAS No. :
產(chǎn)品活性:DTP3 TFA is a potent and selective GADD45β/MKK7 (growth arrest and DNA-damage-inducible β/mitogen-activated protein kinase kinase 7) inhibitor. DTP3 TFA targets an essential, cancer-selective cell-survival module downstream of the NF-κB pathway.
研究領(lǐng)域:Cell Cycle/DNA Damage | MAPK/ERK Pathway
作用靶點:DNA/RNA Synthesis | JNK
In Vitro: DTP3 (10 μM; 1-21 days) causes the potent and tumor-selective induction of JNK activation and apoptosis, as shown by the appearance of phosphorylated JNK, as early as 24 hours.
In Vivo: DTP3 TFA (s.c.; 14.5 mg/kg/day; 28 days) has shown a dramatic shrinkage of the tumors, and virtually eradicates established subcutaneous myeloma xenografts in mice.
DTP3 TFA (intravenous injection; 10 mg/kg/day) has t1/2 of 1.26 hours, CL of 27.13 ML/min/kg, and Vd of 2.80 L/kg.
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